133 related articles for article (PubMed ID: 7633403)
21. Isolation of novel cDNA encompassing the ADU balanced translocation break point in the DiGeorge critical region.
Kim MH; Hur H; Park J; Kim YJ
Mol Biotechnol; 2001 Mar; 17(3):213-7. PubMed ID: 11434309
[TBL] [Abstract][Full Text] [Related]
22. Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome.
Roberts C; Daw SC; Halford S; Scambler PJ
Hum Mol Genet; 1997 Feb; 6(2):237-45. PubMed ID: 9063744
[TBL] [Abstract][Full Text] [Related]
23. GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide.
Gong L; Liu M; Jen J; Yeh ET
Biochim Biophys Acta; 2000 Nov; 1494(1-2):185-8. PubMed ID: 11072084
[TBL] [Abstract][Full Text] [Related]
24. Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene.
McKie JM; Wadey RB; Sutherland HF; Taylor CL; Scambler PJ
Genome Res; 1998 Aug; 8(8):834-41. PubMed ID: 9724329
[TBL] [Abstract][Full Text] [Related]
25. Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.
Pizzuti A; Novelli G; Mari A; Ratti A; Colosimo A; Amati F; Penso D; Sangiuolo F; Calabrese G; Palka G; Silani V; Gennarelli M; Mingarelli R; Scarlato G; Scambler P; Dallapiccola B
Am J Hum Genet; 1996 Apr; 58(4):722-9. PubMed ID: 8644734
[TBL] [Abstract][Full Text] [Related]
26. A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.
Gong W; Emanuel BS; Collins J; Kim DH; Wang Z; Chen F; Zhang G; Roe B; Budarf ML
Hum Mol Genet; 1996 Jun; 5(6):789-800. PubMed ID: 8776594
[TBL] [Abstract][Full Text] [Related]
27. Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome.
Sirotkin H; Morrow B; Saint-Jore B; Puech A; Das Gupta R; Patanjali SR; Skoultchi A; Weissman SM; Kucherlapati R
Genomics; 1997 Jun; 42(2):245-51. PubMed ID: 9192844
[TBL] [Abstract][Full Text] [Related]
28. Molecular characterization of a serine/threonine kinase in the DiGeorge minimal critical region.
Goldmuntz E; Fedon J; Roe B; Budarf ML
Gene; 1997 Oct; 198(1-2):379-86. PubMed ID: 9370305
[TBL] [Abstract][Full Text] [Related]
29. Isolation and characterization of a novel gene deleted in DiGeorge syndrome.
Kurahashi H; Akagi K; Inazawa J; Ohta T; Niikawa N; Kayatani F; Sano T; Okada S; Nishisho I
Hum Mol Genet; 1995 Apr; 4(4):541-9. PubMed ID: 7633402
[TBL] [Abstract][Full Text] [Related]
30. Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans.
Rizzu P; Lindsay EA; Taylor C; O'Donnell H; Levy A; Scambler P; Baldini A
Mamm Genome; 1996 Sep; 7(9):639-43. PubMed ID: 8703114
[TBL] [Abstract][Full Text] [Related]
31. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A
Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926
[TBL] [Abstract][Full Text] [Related]
32. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
[TBL] [Abstract][Full Text] [Related]
33. Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region.
Heisterkamp N; Mulder MP; Langeveld A; ten Hoeve J; Wang Z; Roe BA; Groffen J
Genomics; 1995 Sep; 29(2):451-6. PubMed ID: 8666394
[TBL] [Abstract][Full Text] [Related]
34. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
[TBL] [Abstract][Full Text] [Related]
35. Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).
Schuffenhauer S; Lichtner P; Peykar-Derakhshandeh P; Murken J; Haas OA; Back E; Wolff G; Zabel B; Barisic I; Rauch A; Borochowitz Z; Dallapiccola B; Ross M; Meitinger T
Eur J Hum Genet; 1998; 6(3):213-25. PubMed ID: 9781025
[TBL] [Abstract][Full Text] [Related]
36. The DiGeorge anomaly (CATCH 22, DiGeorge/velocardiofacial syndrome).
Hong R
Semin Hematol; 1998 Oct; 35(4):282-90. PubMed ID: 9801257
[TBL] [Abstract][Full Text] [Related]
37. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
Funke B; Puech A; Saint-Jore B; Pandita R; Skoultchi A; Morrow B
Genomics; 1998 Oct; 53(2):146-54. PubMed ID: 9790763
[TBL] [Abstract][Full Text] [Related]
38. Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.
Sutherland HF; Kim UJ; Scambler PJ
Genomics; 1998 Aug; 52(1):37-43. PubMed ID: 9740669
[TBL] [Abstract][Full Text] [Related]
39. The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.
Gottlieb S; Emanuel BS; Driscoll DA; Sellinger B; Wang Z; Roe B; Budarf ML
Am J Hum Genet; 1997 May; 60(5):1194-201. PubMed ID: 9150167
[TBL] [Abstract][Full Text] [Related]
40. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]